Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6505162
rs6505162
0.050 GeneticVariation BEFREE However, no significant associations were observed in the miR-146a rs2910164 and miR-423 rs6505162 with the susceptibility of ESCC in any genetic model. 31213825

2019

dbSNP: rs6505162
rs6505162
0.050 GeneticVariation BEFREE Logistic regression analyses revealed an association between rs6505162 and ESCC, assuming codominant (AA vs. CC, odds ratios, OR [95% confidence interval, CI]: 0.32 [0.15-0.69], p-value: 0.0076), recessive (AA vs. CC+CA, OR [95% CI]: 0.35 [0.16-0.73], p-value: 0.0027), and log-additive models (OR [95% CI]: 0.69 [0.52-0.91], p-value: 0.0084). 28430524

2017

dbSNP: rs6505162
rs6505162
0.050 GeneticVariation BEFREE A case-control study in 248 Kazakh patients with ESCC and 300 frequency matched control subjects was carried out to examine the potential association of six miRNA (miR-100 rs1834306, miR-34b/c rs4938723, miR-375 rs6715345, miR-146a rs2910164, miR-423 rs6505162 and miR-373 rs12983273) polymorphisms with risk of ESCC. 26261633

2015

dbSNP: rs6505162
rs6505162
0.050 GeneticVariation BEFREE Hsa-miR-423 rs6505162 C>A might associated with a significantly increased risk of ESCC in patients who smoking. 24260422

2013

dbSNP: rs6505162
rs6505162
0.050 GeneticVariation BEFREE In Blacks, rs6505162 A>C was associated with OSCC under dominant, additive and recessive models with odds ratios (ORs) 1.353, 1.404, and 2.858, respectively. 24205249

2013